Canonical Allele Identifier: PA2829600877
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1362265
ClinVar RCV Id: RCV001900092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly75Arg
CA5779384
NM_005343.4:c.223G>A
CA378924583
NM_005343.4:c.223G>C